The Recall Desk
CriticalFDA (Drugs)·D-0639-2019·Announced 2019-03-20

FDA Recalls King Bio Homeopathic Indigestion Relief for Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Indigestion Relief due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

What this means for you

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The agency classification is FDA Class I, which indicates a reasonable probability that use of or exposure to the violative product will cause serious adverse health consequences or death.

Plain-English summary

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Indigestion Relief, 2 fl. oz. (59 mL), due to microbial contamination. The recall involves 479 bottles of the product, identified by NDC 57955-5024-2 and UPC 357955502425.

The affected lots are 052616G (Exp. 05/19), 080315C (Exp. 08/18), and 123016D (Exp. 12/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers should check their inventory for these specific lot numbers and expiration dates. If they possess the recalled product, they should stop using it and contact King Bio Inc. for further instructions or a refund.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Indigestion Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502425, NDC 57955-5024-2
Manufacturer
King Bio Inc.
Affected units
479

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lots: 052616G Exp. 05/19
  • 080315C Exp. 08/18
  • 123016D Exp. 12/19

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 465 recalled by King Bio Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 465 products in this recall →